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191.
有机金属络合物用于高分子富氧膜的研究进展 总被引:2,自引:0,他引:2
本文介绍了能够可逆吸附分子氧的有机金属络合物用于高分子富氧膜的研究进展,以及以双重吸附理论进行的膜的促进输送机理。 相似文献
192.
研究了聚(苯乙烯-丙烯酰胺)(PSAC)载体-氯化钕(NdCl3)络合物对异戊二烯(Ip)聚合的催化行为.PSAC·NdCl3络合物保留了小分子稀土催化剂对双烯烃聚合的催化规律和高度的定向效应.络合物的催化活性随着Nd/Ip和Al/Nd比的增加而增加,所得聚异戊二烯的特性粘数[η]却随之下降.聚异戊二烯的顺式-1,4结构含量达95%.此外,PSAC·NdCl3络合物的活性受PSAC和PSAC·NdCl3的组成与结构的影响.在一定的条件下,络合物的活性随着PSAC中功能团含量的增加而下降.PSAC中单体链节交替分布的程度越低,络合物的活性越高 相似文献
193.
1 INTRODUCTION The donor properties of pyridine N-oxide and its substituted derivatives to form metal complexes have been widely investigated[1~3]. The resulting comple- xes were used as drugs[4] and catalysts[5]. So far, there have been a few reports on the synthesis of Schiff base derived from picolinaldehyde N-oxide with se- micarbazone (PNOS Scheme 1) and its metal com- plexes. And crystal structures of the complexes of PNOS with Au(III)[6], Pd(II)[7] and Cu(II)[8] were re- … 相似文献
194.
The copper(II) complex [Cu(sat)], where Hsat is salicylidene-2-aminothiazole (bidentate Schiff - base), was studied in variety of solvents. In the solid state, the complex is black. It has been characterized by elemental analysis, solubility in common solvents, molar conductivity, and ultraviolet (UV) and visible (Vis) spectroscopy. The complex is easily soluble in common solvents such as chloroform, dimethylformamide, dimethyl sulfoxide, and 1,4-dioxane. The known crystal structure of similar compounds shows planar coordination geometry for the copper center. Combined multitechnique experiments have been applied to confirm the structure of the complex in solutions. The molar conductivities indicate their nonelectrolyte properties in all these solvents. The spectroscopic measurements were used to study the coordination properties of donoratoms and their bonding abilities. 相似文献
195.
含氮宾的两个三核羰基铁簇合物是由[Et_3NH][HFe_3(CO)_(11)]与C_6H_5NCO在苯中反应获得。应用四园衍射仪测定了H_2Fe_3(N-C_6H_5)(CO)_9(Ⅰ)和Fe_3(N-C_6H_5)(μ_3-CO)(CO)_9(Ⅱ)的晶体结构。晶体数据为:C_(15)H_7NO_9Fe_3(Ⅰ),空间群P2_1/a,a=18.343(2),b=9.072(1),c=11.451(1)(?),β=102.03(1)°,V=1863.7(?)~3,Z=4,D_c=2.143g/cm~3;C_(16)H_5NO_(10)Fe_3(Ⅱ),空间群P2_1/c,a=8.634(1),b=13.026(1),c=17.642(2)(?),β=97.68(1)°,V=1966.3(?)~3,Z=4,D_c=1.820g/cm结构系用直接法解出,最后R_(Ⅰ)因子为0.033,R_(Ⅱ)因子为0.027。测定结果表明,(Ⅰ)和(Ⅱ)分子均具有C_s对称性,且三个Fe原子共面,呈近似等边三角形结构。(Ⅰ)中面桥N原子以不对称方式与三个Fe原子成键;(Ⅱ)中面桥羰基以不对称方式与三个Fe原子键连。Fe-N和Fe-C键长分别在1.896-1.938(?)和2.006-2.110(?)之间。 相似文献
196.
Vapor pressure,speciation, and chemical activities in highly concentrated sodium borate solutions at 277 and 317°C 总被引:2,自引:0,他引:2
Oleh Weres 《Journal of solution chemistry》1995,24(5):409-438
The system H2O-B2O3-Na2O has been studied experimentally at 277 and 317°C. The activities of water and boric acid have been determined at mole ratios Na/B from 0 to 1.5, and total dissolved solids 3 to 80 weight percent. The activity of boric acid has been fitted to within experimental error using a speciation model with eight complex species. This model is consistent with the model previously published by Mesmer et al. The electrolyte properties of the liquid are modeled using the Pitzer-Simonson model of very concentrated electrolyte solutions. The calculated values of water activity agree with experiment, and the activity of NaOH and pOH have also been calculated. The potassium borate system also was briefly studied at 317°C, and is adequately described by a model with five complex species. The potassium borate liquid is more alkaline at K/B= 1 than a sodium borate liquid at the same mole ratio, but pOH in the two systems is the same at lower mole ratios. 相似文献
197.
Atsushi Ikeda Masaru Kawaguchi Yoshio Suzuki Tsukasa Hatano Munenori Numata Seiji Shinkai Akio Ohta Makoto Ohta 《Journal of inclusion phenomena and macrocyclic chemistry》2000,38(1-4):163-170
The calixarene-fullerene interaction,which causes only a slight change in the absorptionspectra, has been substantiated by calorimetricmeasurements: the H° values arecomparable with those obtained from the associationconstants estimated by a spectroscopic method. Furthermore, we determined the association constantbetween homooxacalix[3]arene and [60]fullerenederivatives with a porphyrin moiety by fluorescencespectra. 相似文献
198.
The manganese(Ⅲ) complex [Mn(acacen){N(CN)2}]n [H2acacen=bis(acetylacetone)ethylenediimine] has been synthesized and the structure has been determined. The complex forms a one-dimensional chain structure via the bidentate bridge ligand μ1,5-[N(CN)2]- linking [Mn(acacen)] moiety. The magnetic property of the compound (75~300 K) shows the existence of an antiferromagnetic exchange interaction among paramagnetic centers along the chain. CCDC: 244940. 相似文献
199.
0IntroductionThefirstmolecule鄄basedmagnetswerereportedin1986[1].Duringthelasttwodecades,moreandmoreattentionhasbeenpaidtothesynthesisofmolecule鄄basedmagnets,especiallytoPrussianBlueanalogu鄄es[2].TheoldPrussianBlueanalogueshavebeenbroughtuptodateduetoth… 相似文献
200.
IntroductionCertainlanthanideionspossessharpemissionlinesinthevisibleregions.Thepossibilityoftransferringenergyeffi cientlytotheseionsbywayofstronglyabsorbingtransitionscharacteristicoforganicligandshasspurredmanyworkerstoinvestigatelanthanidechelatesaspotentiallasermaterials .Amongthemtheternarycomplexesofeuropium(III)andter bium(III)withtris(β diketonates)andanneutralligandhaveespeciallyattractedmuchattentionfortheirstronglumi nescence.Itmakethemaextensiveapplicationsindevelop mentofnewl… 相似文献